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The liver and the hematolymphoid system: I. The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells

Nylon‐passed spleen cells were found to proliferate when cultured with syngeneic nonparenchymal adherent liver cells and their culture supernatants. The supernatants contained IL‐1, IL‐6, GM‐CSF, and IFN (α + β) activities but not IL‐2 and IL‐3 activities. The IFN level was higher in early culture s...

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Published in:Journal of leukocyte biology 1991-10, Vol.50 (4), p.402-411
Main Authors: Mabuchi, Ayako, Komuro, Toshiro, Saizawa, Takashi, Sakamoto, Toshiki, Watari, Eiji, Yokomuro, Kozo
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container_title Journal of leukocyte biology
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creator Mabuchi, Ayako
Komuro, Toshiro
Saizawa, Takashi
Sakamoto, Toshiki
Watari, Eiji
Yokomuro, Kozo
description Nylon‐passed spleen cells were found to proliferate when cultured with syngeneic nonparenchymal adherent liver cells and their culture supernatants. The supernatants contained IL‐1, IL‐6, GM‐CSF, and IFN (α + β) activities but not IL‐2 and IL‐3 activities. The IFN level was higher in early culture sup (2–24 hr) than in later culture sup (48–72 hr). Proliferation was greatly increased by anti‐IFN (α + β) serum in the spleen cells cultured in the earlier sup. This antiserum increased the spleen cell proliferation only slightly in the later culture sup. This suggests that nonparenchymal liver cells produce two factors, one having a suppressor, and the other an enhancer action, with IFN being one of the suppressor factors. With culture time, DNA synthesis of spleen cells increased and IL‐2 and IL‐3 activities were generated in the culture sup. Cells proliferated during culture were found to be morphologically lymphocytes, granulocytes, and macrophages. The mechanisms by which nonparenchymal liver cells regulate the hematolymphoid system are discussed based on our observations.
doi_str_mv 10.1002/jlb.50.4.402
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The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells</title><source>Alma/SFX Local Collection</source><creator>Mabuchi, Ayako ; Komuro, Toshiro ; Saizawa, Takashi ; Sakamoto, Toshiki ; Watari, Eiji ; Yokomuro, Kozo</creator><creatorcontrib>Mabuchi, Ayako ; Komuro, Toshiro ; Saizawa, Takashi ; Sakamoto, Toshiki ; Watari, Eiji ; Yokomuro, Kozo</creatorcontrib><description>Nylon‐passed spleen cells were found to proliferate when cultured with syngeneic nonparenchymal adherent liver cells and their culture supernatants. The supernatants contained IL‐1, IL‐6, GM‐CSF, and IFN (α + β) activities but not IL‐2 and IL‐3 activities. The IFN level was higher in early culture sup (2–24 hr) than in later culture sup (48–72 hr). Proliferation was greatly increased by anti‐IFN (α + β) serum in the spleen cells cultured in the earlier sup. 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The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells</title><title>Journal of leukocyte biology</title><addtitle>J Leukoc Biol</addtitle><description>Nylon‐passed spleen cells were found to proliferate when cultured with syngeneic nonparenchymal adherent liver cells and their culture supernatants. The supernatants contained IL‐1, IL‐6, GM‐CSF, and IFN (α + β) activities but not IL‐2 and IL‐3 activities. The IFN level was higher in early culture sup (2–24 hr) than in later culture sup (48–72 hr). Proliferation was greatly increased by anti‐IFN (α + β) serum in the spleen cells cultured in the earlier sup. This antiserum increased the spleen cell proliferation only slightly in the later culture sup. This suggests that nonparenchymal liver cells produce two factors, one having a suppressor, and the other an enhancer action, with IFN being one of the suppressor factors. With culture time, DNA synthesis of spleen cells increased and IL‐2 and IL‐3 activities were generated in the culture sup. Cells proliferated during culture were found to be morphologically lymphocytes, granulocytes, and macrophages. The mechanisms by which nonparenchymal liver cells regulate the hematolymphoid system are discussed based on our observations.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Division - physiology</subject><subject>Cells, Cultured</subject><subject>colony‐stimulating factor</subject><subject>Culture Media - analysis</subject><subject>Culture Media - pharmacology</subject><subject>DNA - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - analysis</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - metabolism</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</subject><subject>Immune Sera</subject><subject>Immunobiology</subject><subject>interferon</subject><subject>Interferons - analysis</subject><subject>Interferons - metabolism</subject><subject>Interferons - pharmacology</subject><subject>interleukin</subject><subject>Interleukin-1 - analysis</subject><subject>Interleukin-1 - metabolism</subject><subject>Interleukin-1 - pharmacology</subject><subject>Interleukin-2 - metabolism</subject><subject>Interleukin-3 - metabolism</subject><subject>Interleukin-6 - analysis</subject><subject>Interleukin-6 - metabolism</subject><subject>Interleukin-6 - pharmacology</subject><subject>Kupffer cell</subject><subject>Liver - cytology</subject><subject>Liver - metabolism</subject><subject>Liver - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Miscellaneous</subject><subject>Regulatory factors and their cellular receptors</subject><subject>Spleen - cytology</subject><subject>Spleen - metabolism</subject><subject>Spleen - physiology</subject><subject>Time Factors</subject><issn>0741-5400</issn><issn>1938-3673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhiMEKqVw44rkA3Aiy_gj8W5vUPFRtBKXcracZLxx5djBzrLKT-Jf4iircgPJ0tiaZ-Z9rbcoXlLYUAD2_t41mwo2YiOAPSou6Y5vS15L_ri4BCloWQmAp8WzlO4BgLMaLooLKqmsGb8sft_1SJz9hZFo35Epv3oc9BTcPIx9sB1Jc5pwuCa3G7KwEQ9HpycbPAmG-NkFX446Jczk6BA9adE5MsbgrMG4ks1MdDtlFWJyDTHlNQ71MmRiGLKGP6BH2xIf_Kgj-rafB-3OzpaN6XnxxGiX8MW5XhU_Pn-6u_la7r9_ub35sC9bvtuxUrNGsp1ACQ0FZgwI2bQg2pZpXnPJNXad4QK0EULzLa90vnfM5NOIhtb8qni77s1f-HnENKnBpsWB9hiOSUlGuRSV-C9IawrVli7guxVsY0gpolFjtIOOs6KglghVjlBVoITKEWb81XnvsRmw-wuvmeX-63Nfp1Y7E7VvbXrAKpD1ViwYXbGTdTj_U1J923-EVfrNOtPbQ3-yEVXKKbhshKnT6fRg8Q_51sQJ</recordid><startdate>199110</startdate><enddate>199110</enddate><creator>Mabuchi, Ayako</creator><creator>Komuro, Toshiro</creator><creator>Saizawa, Takashi</creator><creator>Sakamoto, Toshiki</creator><creator>Watari, Eiji</creator><creator>Yokomuro, Kozo</creator><general>Society for Leukocyte Biology</general><general>Federation of American Societies for Experimental Biology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199110</creationdate><title>The liver and the hematolymphoid system: I. The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells</title><author>Mabuchi, Ayako ; Komuro, Toshiro ; Saizawa, Takashi ; Sakamoto, Toshiki ; Watari, Eiji ; Yokomuro, Kozo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3992-a2b7294e70b102ff047bc04cc2a36373aeddf340af44a3835a40ad2fd2fb4b163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Division - physiology</topic><topic>Cells, Cultured</topic><topic>colony‐stimulating factor</topic><topic>Culture Media - analysis</topic><topic>Culture Media - pharmacology</topic><topic>DNA - metabolism</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - analysis</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - metabolism</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</topic><topic>Immune Sera</topic><topic>Immunobiology</topic><topic>interferon</topic><topic>Interferons - analysis</topic><topic>Interferons - metabolism</topic><topic>Interferons - pharmacology</topic><topic>interleukin</topic><topic>Interleukin-1 - analysis</topic><topic>Interleukin-1 - metabolism</topic><topic>Interleukin-1 - pharmacology</topic><topic>Interleukin-2 - metabolism</topic><topic>Interleukin-3 - metabolism</topic><topic>Interleukin-6 - analysis</topic><topic>Interleukin-6 - metabolism</topic><topic>Interleukin-6 - pharmacology</topic><topic>Kupffer cell</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Liver - physiology</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Miscellaneous</topic><topic>Regulatory factors and their cellular receptors</topic><topic>Spleen - cytology</topic><topic>Spleen - metabolism</topic><topic>Spleen - physiology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mabuchi, Ayako</creatorcontrib><creatorcontrib>Komuro, Toshiro</creatorcontrib><creatorcontrib>Saizawa, Takashi</creatorcontrib><creatorcontrib>Sakamoto, Toshiki</creatorcontrib><creatorcontrib>Watari, Eiji</creatorcontrib><creatorcontrib>Yokomuro, Kozo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of leukocyte biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mabuchi, Ayako</au><au>Komuro, Toshiro</au><au>Saizawa, Takashi</au><au>Sakamoto, Toshiki</au><au>Watari, Eiji</au><au>Yokomuro, Kozo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The liver and the hematolymphoid system: I. The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells</atitle><jtitle>Journal of leukocyte biology</jtitle><addtitle>J Leukoc Biol</addtitle><date>1991-10</date><risdate>1991</risdate><volume>50</volume><issue>4</issue><spage>402</spage><epage>411</epage><pages>402-411</pages><issn>0741-5400</issn><eissn>1938-3673</eissn><coden>JLBIE7</coden><abstract>Nylon‐passed spleen cells were found to proliferate when cultured with syngeneic nonparenchymal adherent liver cells and their culture supernatants. The supernatants contained IL‐1, IL‐6, GM‐CSF, and IFN (α + β) activities but not IL‐2 and IL‐3 activities. The IFN level was higher in early culture sup (2–24 hr) than in later culture sup (48–72 hr). Proliferation was greatly increased by anti‐IFN (α + β) serum in the spleen cells cultured in the earlier sup. This antiserum increased the spleen cell proliferation only slightly in the later culture sup. This suggests that nonparenchymal liver cells produce two factors, one having a suppressor, and the other an enhancer action, with IFN being one of the suppressor factors. With culture time, DNA synthesis of spleen cells increased and IL‐2 and IL‐3 activities were generated in the culture sup. Cells proliferated during culture were found to be morphologically lymphocytes, granulocytes, and macrophages. The mechanisms by which nonparenchymal liver cells regulate the hematolymphoid system are discussed based on our observations.</abstract><cop>Bethesda, MD</cop><pub>Society for Leukocyte Biology</pub><pmid>1717623</pmid><doi>10.1002/jlb.50.4.402</doi><tpages>10</tpages></addata></record>
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identifier ISSN: 0741-5400
ispartof Journal of leukocyte biology, 1991-10, Vol.50 (4), p.402-411
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subjects Analysis of the immune response. Humoral and cellular immunity
Animals
Biological and medical sciences
Cell Division - physiology
Cells, Cultured
colony‐stimulating factor
Culture Media - analysis
Culture Media - pharmacology
DNA - metabolism
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Granulocyte-Macrophage Colony-Stimulating Factor - analysis
Granulocyte-Macrophage Colony-Stimulating Factor - metabolism
Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology
Immune Sera
Immunobiology
interferon
Interferons - analysis
Interferons - metabolism
Interferons - pharmacology
interleukin
Interleukin-1 - analysis
Interleukin-1 - metabolism
Interleukin-1 - pharmacology
Interleukin-2 - metabolism
Interleukin-3 - metabolism
Interleukin-6 - analysis
Interleukin-6 - metabolism
Interleukin-6 - pharmacology
Kupffer cell
Liver - cytology
Liver - metabolism
Liver - physiology
Mice
Mice, Inbred C3H
Miscellaneous
Regulatory factors and their cellular receptors
Spleen - cytology
Spleen - metabolism
Spleen - physiology
Time Factors
title The liver and the hematolymphoid system: I. The regulation of nylon-passed spleen cell proliferation by active factors released from syngeneic nonparenchymal liver cells
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